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American Journal of Medical Genetics. Part A
|
April 1, 2004
Slow progression of ataxia-telangiectasia with double missense and in frame splice mutations
Thilo Dörk, Regina Bendix-Waltes, Rolf-Dieter Wegner, et al.
American Journal of Medical Genetics. Part A
|
December 18, 2003
Prenatal diagnosis of fetal trisomy 6 mosaicism and phenotype of the affected newborn
Rolf-Dieter Wegner, Michael Entezami, Ute Knoll, et al.
Prenatal Diagnosis
|
April 21, 2012
'Normal' nuchal translucency: a justification to refrain from detailed scan? Analysis of 6858 cases with special reference to ethical aspects
Rolf Becker, Lothar Schmitz, Stefania Kilavuz, et al.
Prenatal Diagnosis
|
March 1, 2006
Prenatal diagnosis and molecular cytogenetic characterisation of a small de novo interstitial duplication 16q11.2-q13
Marc Trimborn, Rolf-Dieter Wegner, Holger Tönnies, et al.
Prenatal Diagnosis
|
March 3, 2007
Molecular cytogenetic characterisation of an interstitial deletion 12p detected by prenatal diagnosis
Markus Stumm, Eva Klopocki, Adam Gasiorek-Wiens, et al.
Prenatal Diagnosis
|
September 2, 2014
Consanguinity and pregnancy outcomes in a multi-ethnic, metropolitan European population
Rolf Becker, Thomas Keller, Rolf-Dieter Wegner, et al.
Prenatal Diagnosis
|
May 11, 2012
Noninvasive prenatal detection of chromosomal aneuploidies using different next generation sequencing strategies and algorithms
Markus Stumm, Michael Entezami, Nastasja Trunk, et al.
American Journal of Medical Genetics
|
February 22, 2002
Ring chromosome 6 in three fetuses: case reports, literature review, and implications for prenatal diagnosis
Maik Urban, Christiane Bommer, Cornelia Tennstedt, et al.
Journal of Clinical Medicine
|
August 4, 2015
Fetal Aneuploidy Detection by Cell-Free DNA Sequencing for Multiple Pregnancies and Quality Issues with Vanishing Twins
Sebastian Grömminger, Erbil Yagmur, Sanli Erkan, et al.
Journal of the Chinese Medical Association : JCMA
|
May 12, 2010
Small supernumerary marker chromosomes 1 with a normal phenotype
Thomas Liehr, Rolf-Dieter Wegner, Markus Stumm, et al.
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of 2
Search research articles
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Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
American Journal of Medical Genetics. Part A
|
April 1, 2004
Slow progression of ataxia-telangiectasia with double missense and in frame splice mutations
Thilo Dörk, Regina Bendix-Waltes, Rolf-Dieter Wegner, et al.
American Journal of Medical Genetics. Part A
|
December 18, 2003
Prenatal diagnosis of fetal trisomy 6 mosaicism and phenotype of the affected newborn
Rolf-Dieter Wegner, Michael Entezami, Ute Knoll, et al.
Prenatal Diagnosis
|
April 21, 2012
'Normal' nuchal translucency: a justification to refrain from detailed scan? Analysis of 6858 cases with special reference to ethical aspects
Rolf Becker, Lothar Schmitz, Stefania Kilavuz, et al.
Prenatal Diagnosis
|
March 1, 2006
Prenatal diagnosis and molecular cytogenetic characterisation of a small de novo interstitial duplication 16q11.2-q13
Marc Trimborn, Rolf-Dieter Wegner, Holger Tönnies, et al.
Prenatal Diagnosis
|
March 3, 2007
Molecular cytogenetic characterisation of an interstitial deletion 12p detected by prenatal diagnosis
Markus Stumm, Eva Klopocki, Adam Gasiorek-Wiens, et al.
Prenatal Diagnosis
|
September 2, 2014
Consanguinity and pregnancy outcomes in a multi-ethnic, metropolitan European population
Rolf Becker, Thomas Keller, Rolf-Dieter Wegner, et al.
Prenatal Diagnosis
|
May 11, 2012
Noninvasive prenatal detection of chromosomal aneuploidies using different next generation sequencing strategies and algorithms
Markus Stumm, Michael Entezami, Nastasja Trunk, et al.
American Journal of Medical Genetics
|
February 22, 2002
Ring chromosome 6 in three fetuses: case reports, literature review, and implications for prenatal diagnosis
Maik Urban, Christiane Bommer, Cornelia Tennstedt, et al.
Journal of Clinical Medicine
|
August 4, 2015
Fetal Aneuploidy Detection by Cell-Free DNA Sequencing for Multiple Pregnancies and Quality Issues with Vanishing Twins
Sebastian Grömminger, Erbil Yagmur, Sanli Erkan, et al.
Journal of the Chinese Medical Association : JCMA
|
May 12, 2010
Small supernumerary marker chromosomes 1 with a normal phenotype
Thomas Liehr, Rolf-Dieter Wegner, Markus Stumm, et al.
Page
of 2